Potassium Carbonate → 6-Methoxy-7-(3-morpholinopropoxy)-4-(quinolin-5-yloxy)-quinazoline

HRID 1791684ノート

反応式

HRID 1791684 の反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH2:15][CH2:16][CH2:17][N:18]3[CH2:23][CH2:22][O:21][CH2:20][CH2:19]3)=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].[OH:30][C:31]1[CH:40]=[CH:39][CH:38]=[C:37]2[C:32]=1[CH:33]=[CH:34][CH:35]=[N:36]2.[OH-].[Na+]>CN(C=O)C>[CH3:13][O:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][C:8]=1[O:14][CH2:15][CH2:16][CH2:17][N:18]1[CH2:23][CH2:22][O:21][CH2:20][CH2:19]1)[N:5]=[CH:4][N:3]=[C:2]2[O:30][C:31]1[CH:40]=[CH:39][CH:38]=[C:37]2[C:32]=1[CH:33]=[CH:34][CH:35]=[N:36]2

参加物

6

反応物 4

HCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 118239414-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolineHCID 135441757Quinolin-5-ol

生成物 1

HCID 220305986-Methoxy-7-(3-morpholinopropoxy)-4-(quinolin-5-yloxy)-quinazoline収率 59.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

A mixture of 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (225 mg, 0.67 mmol), (prepared as described for the starting material in Example 1), potassium carbonate (106 mg, 0.77 mmol) and 5-hydroxyquinoline (111 mg, 0.77 mmol) in DMF (7.5 ml) was stirred at 100° C. for 5 hours and allowed to cool to ambient temperature. The reaction mixture was treated with 1.0 N aqueous sodium hydroxide solution (40 ml) and allowed to stir at ambient temperature for a few minutes. The resulting precipitate was filtered off, washed with water and air dried for a short while. The damp solid was dissolved in dichloromethane, filtered through phase separating paper and the filtrate evaporated under vacuum. The residue was triturated with ether, filtered and dried to give 6-methoxy-7-(3-morpholinopropoxy)-4-(quinolin-5-yloxy)-quinazoline (178 mg, 59%).

後処理

  1. custom(prepared
  2. temperatureto cool to ambient temperature
  3. stirringto stir at ambient temperature for a few minutes
  4. filtrationThe resulting precipitate was filtered off
  5. washwashed with water and air
  6. customdried for a short while
  7. dissolutionThe damp solid was dissolved in dichloromethane
  8. filtrationfiltered through phase
  9. customseparating paper
  10. customthe filtrate evaporated under vacuum
  11. customThe residue was triturated with ether
  12. filtrationfiltered
  13. customdried

出典と根拠

ORDレコード
ord-e4ec6c08da654f7997c0a4f544c47d32
出典データセット
uspto-grants-2006_07
特許番号
US07074800B1

反応ノート

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